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The inhibitory effect of N-p-chlorobenzenesulfonyl-4-aminosalicylic acid on dextran sodium sulfate-induced ulcerative colitis
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Xue-qin ZHOU1, Chang SU1, Xiao-tong LI1, Xue-min YU1, Shu-wan QI1, Tao LIU2, Jing-mei ZHANG3, Jing YAO4, *
Acta Pharmaceutica Sinica | 2018, 53(10) : 1652 - 1659
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Acta Pharmaceutica Sinica | 2018, 53(10): 1652-1659
ORIGINAL ARTICLES
The inhibitory effect of N-p-chlorobenzenesulfonyl-4-aminosalicylic acid on dextran sodium sulfate-induced ulcerative colitis
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Xue-qin ZHOU1, Chang SU1, Xiao-tong LI1, Xue-min YU1, Shu-wan QI1, Tao LIU2, Jing-mei ZHANG3, Jing YAO4, *
Affiliations
  • 1. School of Clinical Medicine, Jining Medical University, Jining 272067, China
  • 2. Affiliated Hospital, Jining Medical University, Jining 272067, China
  • 3. Institute of Behavioral Medicine Education, Jining Medical University, Jining 272067, China
  • 4. School of Basic Medicine, Jining Medical University, Jining 272067, China
Published: 2018-10-12 doi: 10.16438/j.0513-4870.2018-0567
Outline
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The study aims to explore the effects of N-p--chlorobenzenesulfonyl-4-amino salicylic acid on the dextran sodium sulfate (DSS)-induced ulcerative colitis in mouse. A total of 60 BALB/c mice were randomly divided into 6 groups (n=10):control group, DSS model group, 5-amino salicylic acid (5-ASA) group, and administration groups (N-p--chlorobenzenesulfonyl-4-aminosalicylic acid) 10, 20, 40 mg·kg-1. Model group were induced by drinking 4% (w/v) DSS solution for 7 days and normal water for the next 3 days. The positive group and drug group mouse were given 5-ASA (40 mg·kg-1) and N-p--chlorobenzene sulfonyl-4-amino salicylic acid (10, 20, 40 mg·kg-1) by gavage respectively. During the experiment, changes in body weight, bloody stool, fecal character and mental status were observed daily. Damage and repair of the colon mucosa and the pathological changes of important organs were observed by hematoxylin and eosin (HE) staining. Expression of inflammatory factors such as tumor necrosis factor alpha (TNF-α), interleukin 1 beta (IL-1β), interleukin 6 (IL-6), macrophage inflammatory protein 2 (MIP-2), myeloperoxidase (MPO) in serum were detected by ELISA. The results showed that bloody stools and diarrhea emerged on the 4th day after model establishment in model mice. The number of bloody mice rose to ten, and blood and diarrhea began to appear in the administration group on the 7th day. Mental status was poor and body weight decreased significantly in model group since the 4th day, and the situation was improved in the administration group and 5-ASA group. Colons in the administration groups (10, 20, 40 mg·kg-1) were longer than those in the DSS model group. In the DSS model group, the colonic mucosa and submucosa of mice exhibited severe inflammatory cell infiltration, various degrees of necrosis, proliferation. In the middle dose group (20 mg·kg-1), the situation has improved slightly and the colonic mucosa showed mildly chronic inflammation and a small amount of inflammatory cells infiltration. The high dose group (40 mg·kg-1) showed normal colon mucosal, relatively complete epithelial structure and few inflammatory cell infiltration. The levels of IL-1β, IL-6, TNF-α, MIP-2 and MPO in the serum of mice were lower in the administration group (40 mg·kg-1) than in model group. Therefore, N-p--chlorobenzenesulfonyl-4-amino salicylic acid might be a feasible treatment for DSS-induced UC.

N-p--chlorobenzenesulfonyl-4-amino salicylic acid  /  dextran sodium sulfate  /  ulcerative colitis  /  inflammatory factor  /  macrophage inflammatory protein 2  /  myeloperoxidase
Xue-qin ZHOU, Chang SU, Xiao-tong LI, Xue-min YU, Shu-wan QI, Tao LIU, Jing-mei ZHANG, Jing YAO. The inhibitory effect of N-p-chlorobenzenesulfonyl-4-aminosalicylic acid on dextran sodium sulfate-induced ulcerative colitis[J]. Acta Pharmaceutica Sinica, 2018 , 53 (10) : 1652 -1659 . DOI: 10.16438/j.0513-4870.2018-0567
Year 2018 volume 53 Issue 10
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Article Info
doi: 10.16438/j.0513-4870.2018-0567
  • Receive Date:2018-06-18
  • Online Date:2026-01-15
  • Published:2018-10-12
Article Data
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History
  • Received:2018-06-18
  • Revised:2018-07-26
Funding
Affiliations
    1. School of Clinical Medicine, Jining Medical University, Jining 272067, China
    2. Affiliated Hospital, Jining Medical University, Jining 272067, China
    3. Institute of Behavioral Medicine Education, Jining Medical University, Jining 272067, China
    4. School of Basic Medicine, Jining Medical University, Jining 272067, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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